510(k) K073096
K073096 is an FDA 510(k) premarket notification submitted by Epitek, Inc. for the device "ANCHORAGE CLOSURE DEVICE". The FDA issued a decision of Substantially Equivalent on February 7, 2008. The device falls under product code GAT (Suture, Nonabsorbable, Synthetic, Polyethylene), a Class II device regulated under 21 CFR 878.5000. Epitek, Inc. has at least 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 7, 2008
- Date Received
- November 1, 2007
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Suture, Nonabsorbable, Synthetic, Polyethylene
- Device Class
- Class II
- Regulation Number
- 878.5000
- Review Panel
- SU
- Submission Type